Canonical Allele Identifier: CA805689413

Gene: LPCAT1

Linked Data

• dbSNP Id: rs1239982200
• gnomAD v3: 5-1518381-C-T
• gnomAD v4: 5-1518381-C-T
• MyVariant Identifiers: chr5:g.1518496C>T (hg19) ; chr5:g.1518381C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1518381C>T , CM000667.2:g.1518381C>T	GRCh38
NC_000005.9:g.1518496C>T , CM000667.1:g.1518496C>T	GRCh37
NC_000005.8:g.1571496C>T	NCBI36
NG_051622.1:g.10597G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283415.4:c.135+5329G>A MANE Select	ENSP00000283415.3:n.135+5329G>A
ENST00000283415.3:c.135+5329G>A	ENSP00000283415.3:n.135+5329G>A
ENST00000475622.5:c.135+5329G>A	ENSP00000423472.1:n.135+5329G>A
ENST00000514484.6:n.165+2966G>A
NM_024830.3:c.135+5329G>A	NP_079106.3:n.135+5329G>A
XM_005248373.2:c.-10+2966G>A	XP_005248430.1:n.-10+2966G>A
XM_011514133.1:c.201+7134G>A	XP_011512435.1:n.201+7134G>A
NM_024830.4:c.135+5329G>A	NP_079106.3:n.135+5329G>A
XM_005248373.3:c.-10+2966G>A	XP_005248430.1:n.-10+2966G>A
NM_024830.5:c.135+5329G>A MANE Select	NP_079106.3:n.135+5329G>A